Variant #0000074053 (NC_000013.10:g.(31835220_31843350)_(31905653_?)del, NC_000013.10(NM_194318.3):c.(596+1_597-1)_(*1848_?)del (B3GLCT))
Chromosome |
13 |
Allele |
Maternal (confirmed) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(31835220_31843350)_(31905653_?)del |
DNA change (hg38) |
- |
Published as |
(?_-142)_(*1848_?)del |
ISCN |
- |
DB-ID |
B3GLCT_000001 See all 2 reported entries |
Variant remarks |
partial gene deletion (exon 8-15), not as reported a full gene deletion |
Reference |
PubMed: Lesnik Oberstein 2006, PubMed: Hess 2008 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Martine van Belzen |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2006-08-10 16:30:52 +02:00 (CEST) |
Date last edited |
2011-08-19 17:44:09 +02:00 (CEST) |

Variant on transcripts
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